Catherine Dauga , Valentine Gilbart , Azimdine Habib , Laura Tondeur , Rindra Randremanana , Boris Hedible , Alexandre Manirazika , Muriel Vray , Ronan Jambou , the Malinea Clinical Trial Group
{"title":"三个非洲国家儿童肠道菌群多样性","authors":"Catherine Dauga , Valentine Gilbart , Azimdine Habib , Laura Tondeur , Rindra Randremanana , Boris Hedible , Alexandre Manirazika , Muriel Vray , Ronan Jambou , the Malinea Clinical Trial Group","doi":"10.1016/j.meegid.2025.105808","DOIUrl":null,"url":null,"abstract":"<div><div>In children, the gut microbiota is a dynamic ecosystem derived from breastfeeding, oral microbiota and diet. Diversity can vary from one country to another, and the aim of this study was to compare microbiota of well-nourished children between three African countries using fully standardized protocols from sampling to data analysis.</div><div>Well-nourished (WHZ weight for height z-score ≥ −1.5) children aged 18–24 months were enrolled. Libraries were constructed using Illumina 16S protocol. Sequences were aligned to the Silva.nr and clustered into OTUs (organism taxonomic unit) using greedy clustering (dgc). Consensus determination was done using classify.otu and the OTU table, taxonomy and metadata were assembled using Phyloseq. Alpha diversity was assessed using Chao1, Shannon and Simpson's index using Mothur.</div><div>106 well-nourished children were selected (31 in Madagascar, 40 in Senegal and 35 in Centrafrican Republic CAR). Richness was higher in Senegal than in CAR or Madagascar, but diversity was lowest in Senegal and highest in CAR. As the quality of drinking water increased, richness increased and diversity decreased. Microbiota shared five dominant phyla in different proportions: <em>Firmicutes, Bacteroidetes, Proteobacteria, Actinobacteria, Verrucomicrobia</em>. The composition of the microbiota in Madagascar and Centrafrica republic (CAR) was more similar, with more <em>Prevotella 9</em> in Madagascar and more <em>Bifidobacterium</em> in CAR. Only two taxa were markers from CAR (<em>Prevotella 9</em> and <em>Ruminococcus 2</em>).</div><div>Apart from a pool of common species, a large proportion of rare species may characterize each geographical context. Therefore, the microbiota of children in Africa cannot be considered comparable between countries. Each biotope harbors specific species on a common background.</div></div>","PeriodicalId":54986,"journal":{"name":"Infection Genetics and Evolution","volume":"134 ","pages":"Article 105808"},"PeriodicalIF":2.6000,"publicationDate":"2025-08-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Intestinal microbiota diversity in children from three African countries\",\"authors\":\"Catherine Dauga , Valentine Gilbart , Azimdine Habib , Laura Tondeur , Rindra Randremanana , Boris Hedible , Alexandre Manirazika , Muriel Vray , Ronan Jambou , the Malinea Clinical Trial Group\",\"doi\":\"10.1016/j.meegid.2025.105808\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>In children, the gut microbiota is a dynamic ecosystem derived from breastfeeding, oral microbiota and diet. Diversity can vary from one country to another, and the aim of this study was to compare microbiota of well-nourished children between three African countries using fully standardized protocols from sampling to data analysis.</div><div>Well-nourished (WHZ weight for height z-score ≥ −1.5) children aged 18–24 months were enrolled. Libraries were constructed using Illumina 16S protocol. Sequences were aligned to the Silva.nr and clustered into OTUs (organism taxonomic unit) using greedy clustering (dgc). Consensus determination was done using classify.otu and the OTU table, taxonomy and metadata were assembled using Phyloseq. Alpha diversity was assessed using Chao1, Shannon and Simpson's index using Mothur.</div><div>106 well-nourished children were selected (31 in Madagascar, 40 in Senegal and 35 in Centrafrican Republic CAR). Richness was higher in Senegal than in CAR or Madagascar, but diversity was lowest in Senegal and highest in CAR. As the quality of drinking water increased, richness increased and diversity decreased. Microbiota shared five dominant phyla in different proportions: <em>Firmicutes, Bacteroidetes, Proteobacteria, Actinobacteria, Verrucomicrobia</em>. The composition of the microbiota in Madagascar and Centrafrica republic (CAR) was more similar, with more <em>Prevotella 9</em> in Madagascar and more <em>Bifidobacterium</em> in CAR. Only two taxa were markers from CAR (<em>Prevotella 9</em> and <em>Ruminococcus 2</em>).</div><div>Apart from a pool of common species, a large proportion of rare species may characterize each geographical context. Therefore, the microbiota of children in Africa cannot be considered comparable between countries. 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Intestinal microbiota diversity in children from three African countries
In children, the gut microbiota is a dynamic ecosystem derived from breastfeeding, oral microbiota and diet. Diversity can vary from one country to another, and the aim of this study was to compare microbiota of well-nourished children between three African countries using fully standardized protocols from sampling to data analysis.
Well-nourished (WHZ weight for height z-score ≥ −1.5) children aged 18–24 months were enrolled. Libraries were constructed using Illumina 16S protocol. Sequences were aligned to the Silva.nr and clustered into OTUs (organism taxonomic unit) using greedy clustering (dgc). Consensus determination was done using classify.otu and the OTU table, taxonomy and metadata were assembled using Phyloseq. Alpha diversity was assessed using Chao1, Shannon and Simpson's index using Mothur.
106 well-nourished children were selected (31 in Madagascar, 40 in Senegal and 35 in Centrafrican Republic CAR). Richness was higher in Senegal than in CAR or Madagascar, but diversity was lowest in Senegal and highest in CAR. As the quality of drinking water increased, richness increased and diversity decreased. Microbiota shared five dominant phyla in different proportions: Firmicutes, Bacteroidetes, Proteobacteria, Actinobacteria, Verrucomicrobia. The composition of the microbiota in Madagascar and Centrafrica republic (CAR) was more similar, with more Prevotella 9 in Madagascar and more Bifidobacterium in CAR. Only two taxa were markers from CAR (Prevotella 9 and Ruminococcus 2).
Apart from a pool of common species, a large proportion of rare species may characterize each geographical context. Therefore, the microbiota of children in Africa cannot be considered comparable between countries. Each biotope harbors specific species on a common background.
期刊介绍:
(aka Journal of Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases -- MEEGID)
Infectious diseases constitute one of the main challenges to medical science in the coming century. The impressive development of molecular megatechnologies and of bioinformatics have greatly increased our knowledge of the evolution, transmission and pathogenicity of infectious diseases. Research has shown that host susceptibility to many infectious diseases has a genetic basis. Furthermore, much is now known on the molecular epidemiology, evolution and virulence of pathogenic agents, as well as their resistance to drugs, vaccines, and antibiotics. Equally, research on the genetics of disease vectors has greatly improved our understanding of their systematics, has increased our capacity to identify target populations for control or intervention, and has provided detailed information on the mechanisms of insecticide resistance.
However, the genetics and evolutionary biology of hosts, pathogens and vectors have tended to develop as three separate fields of research. This artificial compartmentalisation is of concern due to our growing appreciation of the strong co-evolutionary interactions among hosts, pathogens and vectors.
Infection, Genetics and Evolution and its companion congress [MEEGID](http://www.meegidconference.com/) (for Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases) are the main forum acting for the cross-fertilization between evolutionary science and biomedical research on infectious diseases.
Infection, Genetics and Evolution is the only journal that welcomes articles dealing with the genetics and evolutionary biology of hosts, pathogens and vectors, and coevolution processes among them in relation to infection and disease manifestation. All infectious models enter the scope of the journal, including pathogens of humans, animals and plants, either parasites, fungi, bacteria, viruses or prions. The journal welcomes articles dealing with genetics, population genetics, genomics, postgenomics, gene expression, evolutionary biology, population dynamics, mathematical modeling and bioinformatics. We also provide many author benefits, such as free PDFs, a liberal copyright policy, special discounts on Elsevier publications and much more. Please click here for more information on our author services .